Ishida Hiroyuki, Adachi Souichi, Hasegawa Daiichiro, Okamoto Yasuhiro, Goto Hiroaki, Inagaki Jiro, Inoue Masami, Koh Katsuyoshi, Yabe Hiromasa, Kawa Keisei, Kato Koji, Atsuta Yoshiko, Kudo Kazuko
Department of Pediatrics, Kyoto Prefectural University of Medicine, Kyoto, Japan; Division of Pediatrics, Matsushita Memorial Hospital, Moriguchi, Japan.
Pediatr Blood Cancer. 2015 May;62(5):883-9. doi: 10.1002/pbc.25389. Epub 2014 Dec 24.
The relative efficacy of allogeneic hematopoietic cell transplantation (allo-HCT) after reduced toxicity conditioning (RTC) compared with standard myeloablative conditioning (MAC) in pediatric patients with acute myeloid leukemia (AML) has not been studied extensively. To address whether RTC is a feasible approach for pediatric patients with AML in remission, we performed a retrospective investigation of the outcomes of the first transplant in patients who had received an allo-HCT after RTC or standard MAC, using nationwide registration data collected between 2000 and 2011 in Japan.
We compared a fludarabine (Flu) and melphalan (Mel)-based regimen (RTC; n = 34) with total body irradiation (TBI) and/or busulfan (Bu)-based conditioning (MAC; n = 102) in demographic- and disease-criteria-matched childhood and adolescent patients with AML in first or second complete remission (CR1/CR2).
The incidence of engraftment, early complications, grade II-IV acute graft-versus-host disease (GVHD), and chronic GVHD were similar in each conditioning group. The risk of relapse (25% vs. 26%) and non-relapse mortality (13% vs. 11%) after 3 years did not differ between these groups, and univariate and multivariate analyses demonstrated that the 3-year overall survival (OS) rates after Flu/Mel-RTC and MAC were comparable (mean, 72% [range, 51-85%] and 68% [range, 58-77%], respectively).
The results suggest that the Flu/Mel-RTC regimen is a clinically acceptable conditioning strategy for childhood and adolescent patients with AML in remission. Although this retrospective, registry-based analysis has several limitations, RTC deserves to be further investigated in prospective trials.
在急性髓系白血病(AML)患儿中,与标准清髓性预处理(MAC)相比,减低毒性预处理(RTC)后进行异基因造血细胞移植(allo-HCT)的相对疗效尚未得到广泛研究。为了探讨RTC是否是处于缓解期的AML患儿的一种可行方法,我们利用2000年至2011年期间在日本收集的全国登记数据,对接受RTC或标准MAC后进行allo-HCT的患者首次移植的结局进行了回顾性调查。
我们在年龄和疾病标准匹配的首次或第二次完全缓解(CR1/CR2)的儿童和青少年AML患者中,比较了基于氟达拉滨(Flu)和马法兰(Mel)的预处理方案(RTC;n = 34)与基于全身照射(TBI)和/或白消安(Bu)的预处理方案(MAC;n = 102)。
每个预处理组的植入率、早期并发症、II-IV级急性移植物抗宿主病(GVHD)和慢性GVHD的发生率相似。两组之间3年后的复发风险(25%对26%)和非复发死亡率(13%对11%)没有差异,单因素和多因素分析表明,Flu/Mel-RTC和MAC后的3年总生存率(OS)相当(平均分别为72%[范围51 - 85%]和68%[范围58 - 77%])。
结果表明,Flu/Mel-RTC方案对于处于缓解期的儿童和青少年AML患者是一种临床上可接受的预处理策略。尽管这项基于登记数据的回顾性分析有几个局限性,但RTC值得在前瞻性试验中进一步研究。